| Term Name: | Parkinson's disease 22 |
|---|---|
| Synonyms: | autosomal dominant Parkinson's disease 22 |
| Definition: | A late onset Parkinson's disease that has_material_basis_in autosomal dominant inheritance of heterozygous mutation in the coiled-coil-helix-coiled-coil-helix domain containing 2 gene on chromosome 7p11.2. |
| Ontology: | Human Disease [DOID:0080504] ( DOID:0080504 ) |